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1.
Bocher, O. et al.: Disentangling the consequences of type 2 diabetes on targeted metabolite profiles using causal inference and interaction QTL analyses. PLoS Genet. 20:e1011346 (2024)
2.
Kerimov, N.* et al.: eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs. PLoS Genet. 19:e1010932 (2023)
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Bocher, O. et al.: Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score. PLoS Genet. 18:e1009923 (2022)
4.
Butler-Laporte, G.* et al.: Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. PLoS Genet. 18:e1010367 (2022)
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Milenkovic, D.* et al.: Mice lacking the mitochondrial exonuclease MGME1 develop inflammatory kidney disease with glomerular dysfunction. PLoS Genet. 18:e1010190 (2022)
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Albanese, M. et al.: MicroRNAs are minor constituents of extracellular vesicles that are rarely delivered to target cells. PLoS Genet. 17:e1009951 (2021)
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Böck, J.* et al.: Human genome diversity data reveal that L564P is the predominant TPC2 variant and a prerequisite for the blond hair associated M484L gain-of-function effect. PLoS Genet. 17:e1009236 (2021)
8.
Goveas, N.* et al.: MLL1 is required for maintenance of intestinal stem cells. PLoS Genet. 17:e1009250 (2021)
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Swan, A.L.* et al.: Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density. PLoS Genet. 16:e1009190 (2021)
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Haeussler, S.* et al.: Autophagy compensates for defects in mitochondrial dynamics. PLoS Genet. 16:e1008638 (2020)
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Reza Sailani, M.* et al.: Candidate variants in TUB are associated with familial tremor. PLoS Genet. 16:e1009010 (2020)
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Riveros-McKay, F.* et al.: The influence of rare variants in circulating metabolic biomarkers. PLoS Genet. 16:e1008605 (2020)
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Vogelezang, S.* et al.: Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits. PLoS Genet. 16:e1008718 (2020)
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Zhang, T.* et al.: High-throughput discovery of genetic determinants of circadian misalignment. PLoS Genet. 16:e1008577 (2020)
15.
Rivas, M.A.* et al.: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 14:e1007329 (2018)
16.
Graff, M.* et al.: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults. PLoS Genet. 13:e1006528 (2017)
17.
Magosi, L.E.* ; Goel, A.* ; Hopewell, J.C.* ; Farrall, M.* & CARDIoGRAMplusC4D Consortium (Gieger, C. ; Peters, A. ; Meitinger, T.): Identifying systematic heterogeneity patterns in genetic association meta-analysis studies. PLoS Genet. 13:e1006755 (2017)
18.
Scahill, C.M.* et al.: Loss of the chromatin modifier Kdm2aa causes BrafV-600E -independent spontaneous melanoma in zebrafish. PLoS Genet. 13:e1006959 (2017)
19.
Shungin, D.* et al.: Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLoS Genet. 13:e1006812 (2017)
20.
Wagner, G.* et al.: Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition. PLoS Genet. 13:e1006757 (2017)
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